کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
6157394 | 1598251 | 2015 | 11 صفحه PDF | دانلود رایگان |
عنوان انگلیسی مقاله ISI
Research Priorities in CKD: Report of a National Workshop Conducted in Australia
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کلمات کلیدی
Quality of life - کیفیت زندگیChronic kidney disease (CKD) - بیماری مزمن کلیه (CKD)Clinical research - تحقیقات بالینیResource allocation - تخصیص منابعPriority setting - تعیین اولویتrenal replacement therapy - درمان جایگزینی کلیهStakeholder - ذی نفعPatient - صبورCaregiver - مراقبPatient-centered care - مراقبت از بیمار محورResearch - پژوهش یا تحقیقDisease prevention - پیشگیری از بیماریHealth care worker - کارمند بهداشت و درمان
موضوعات مرتبط
علوم پزشکی و سلامت
پزشکی و دندانپزشکی
بیماریهای کلیوی
پیش نمایش صفحه اول مقاله
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چکیده انگلیسی
Research aims to improve health outcomes for patients. However, the setting of research priorities is usually performed by clinicians, academics, and funders, with little involvement of patients or caregivers and using processes that lack transparency. A national workshop was convened in Australia to generate and prioritize research questions in chronic kidney disease (CKD) among diverse stakeholder groups. Patients with CKD (n = 23), nephrologists/surgeons (n = 16), nurses (n = 8), caregivers (n = 7), and allied health professionals and researchers (n = 4) generated and voted on intervention questions across 4 treatment categories: CKD stages 1 to 5 (non-dialysis dependent), peritoneal dialysis, hemodialysis, and kidney transplantation. The 5 highest ranking questions (in descending order) were as follows: How effective are lifestyle programs for preventing deteriorating kidney function in early CKD? What strategies will improve family consent for deceased donor kidney donation, taking different cultural groups into account? What interventions can improve long-term post-transplant outcomes? What are effective interventions for post hemodialysis fatigue? How can we improve and individualize drug therapy to control post-transplant side effects? Priority questions were focused on prevention, lifestyle, quality of life, and long-term impact. These prioritized research questions can inform funding agencies, patient/consumer organizations, policy makers, and researchers in developing a CKD research agenda that is relevant to key stakeholders.
ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: American Journal of Kidney Diseases - Volume 66, Issue 2, August 2015, Pages 212-222
Journal: American Journal of Kidney Diseases - Volume 66, Issue 2, August 2015, Pages 212-222
نویسندگان
Allison PhD, Sally PG Dip, Shingisai MPH, Alan PhD, Steve J. PhD, Jeremy R. FRCP, Martin PhD, Carmel M. MBBS, Sophie PhD, Kirsten PhD, David W. PhD, Peter G. PhD, Anne McKenzie, David Parker, Vlado PhD, Kevan R. PhD, Carol PhD, Giovanni F.M. PhD,